Class II

Medical Device Recall: Halyard EYE PACK. Model/Catalog Number: LVEY27 Convenience kit.

AVID Medical, Inc. · May 7, 2026

Reason for Recall

Incorrect concentration of Betadine solution contained within certain AVID convenience kits.

Distribution

US Nationwide distribution in the state of California.

States Affected

NATIONWIDE

Quantity Affected

260 kits

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2763-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

AVID Medical, Inc. Medical Device Recall: Halyard EYE PACK. Model/Catalog Number: LVEY27 Convenience kit. | SafeCheck